Efficacy and Safety of Minocycline in Patients With Acute Ischaemic Stroke Receiving Intravenous Thrombolysis

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-80
SponsorBeijing Tiantan Hospital

About this trial

The aim of this study is to assess the efficacy and safety of minocycline in improving functional outcome among patients with acute ischaemic stroke receiving intravenous thrombolysis.

Eligibility criteria

Qualifiers

Age between 18 and 80 years;

Patients with acute ischaemic stroke confirmed by CT or MRI;

Having received or planning to receive intravenous thrombolysis within 4.5 hours of onset or within an extended window of 4.5-24 hours based on guideline recommendations (The intravenous thrombolytic drugs include: alteplase, tenecteplase, reteplase or recombinant human prourokinase);

The study drug can be applied before intravenous thrombolysis or within 2 hours after the initiation of intravenous thrombolysis;

Disqualifiers

mRS score ≥ 2 prior to onset of the current stroke;

History of pseudomembranous colitis or antibiotic-associated colitis;

Known allergy or intolerance to tetracycline antibiotics or any component of minocycline;

Known resistance to other tetracyclines;

Trial design

Treatments tested in this trial

  • Minocycline Hydrochloride Capsule (50 mg per capsule)
  • Placebo of Minocycline Hydrochloride Capsule (50 mg per capsule, containing 0 mg of minocycline)

Treatment groups

934 Participants
are divided into 2 treatment groups

Sponsors and collaborators